Canonical Allele Identifier: CA10614494

Gene: PAX3

Linked Data

• ClinVar Variation Id: 334557
• ClinVar RCV Id: RCV000262533 ; RCV000357449
• dbSNP Id: rs886055675
• gnomAD v2: 2-223066854-T-A
• gnomAD v3: 2-222202135-T-A
• gnomAD v4: 2-222202135-T-A
• MyVariant Identifiers: chr2:g.223066854T>A (hg19) ; chr2:g.222202135T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222202135T>A , CM000664.2:g.222202135T>A	GRCh38
NC_000002.11:g.223066854T>A , CM000664.1:g.223066854T>A	GRCh37
NC_000002.10:g.222775098T>A	NCBI36
NG_011632.1:g.101847A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336840.11:c.1174-693A>T	ENSP00000338767.5:n.1174-693A>T
ENST00000344493.9:c.1174-693A>T	ENSP00000342092.4:n.1174-693A>T
ENST00000350526.9:c.1229A>T	ENSP00000343052.4:p.Tyr410Phe
ENST00000392070.7:c.1229A>T MANE Select	ENSP00000375922.3:p.Tyr410Phe
ENST00000464706.6:n.667A>T
ENST00000644699.1:n.555A>T
ENST00000646154.1:n.1043A>T
ENST00000336840.10:c.1174-693A>T	ENSP00000338767.5:n.1174-693A>T
ENST00000344493.8:c.1174-693A>T	ENSP00000342092.4:n.1174-693A>T
ENST00000350526.8:c.1229A>T	ENSP00000343052.4:p.Tyr410Phe
ENST00000392069.6:c.1229A>T	ENSP00000375921.2:p.Tyr410Phe
ENST00000392070.6:c.1229A>T	ENSP00000375922.2:p.Tyr410Phe
ENST00000409551.7:c.1226A>T	ENSP00000386750.3:p.Tyr409Phe
ENST00000464706.5:n.653A>T
NM_001127366.2:c.1226A>T	NP_001120838.1:p.Tyr409Phe
NM_181457.3:c.1229A>T	NP_852122.1:p.Tyr410Phe
NM_181458.3:c.1229A>T	NP_852123.1:p.Tyr410Phe
NM_181459.3:c.1229A>T	NP_852124.1:p.Tyr410Phe
NM_181460.3:c.1174-693A>T	NP_852125.1:n.1174-693A>T
NM_181461.3:c.1174-693A>T	NP_852126.1:n.1174-693A>T
XM_011511278.1:c.1373A>T	XP_011509580.1:p.Tyr458Phe
XM_011511279.1:c.665A>T	XP_011509581.1:p.Tyr222Phe
NM_001127366.3:c.1226A>T	NP_001120838.1:p.Tyr409Phe
NM_181457.4:c.1229A>T	NP_852122.1:p.Tyr410Phe
NM_181458.4:c.1229A>T MANE Select	NP_852123.1:p.Tyr410Phe
NM_181459.4:c.1229A>T	NP_852124.1:p.Tyr410Phe
NM_181460.4:c.1174-693A>T	NP_852125.1:n.1174-693A>T
NM_181461.4:c.1174-693A>T	NP_852126.1:n.1174-693A>T